Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP946386.RAB-KCVZ1nJzrF5KJmtv7S_-YHMTlzHmwvjX900gbFTxg130_assertion> ?p ?o ?g. }
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- NP946386.RAB-KCVZ1nJzrF5KJmtv7S_-YHMTlzHmwvjX900gbFTxg130_assertion type Assertion NP946386.RAB-KCVZ1nJzrF5KJmtv7S_-YHMTlzHmwvjX900gbFTxg130_head.
- NP946386.RAB-KCVZ1nJzrF5KJmtv7S_-YHMTlzHmwvjX900gbFTxg130_assertion description "[In one of the patients, the PRKAR1A gene responsible for Carney Complex and the KCNJ2 gene causal for Andersen syndrome are deleted.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP946386.RAB-KCVZ1nJzrF5KJmtv7S_-YHMTlzHmwvjX900gbFTxg130_provenance.
- NP946386.RAB-KCVZ1nJzrF5KJmtv7S_-YHMTlzHmwvjX900gbFTxg130_assertion evidence source_evidence_literature NP946386.RAB-KCVZ1nJzrF5KJmtv7S_-YHMTlzHmwvjX900gbFTxg130_provenance.
- NP946386.RAB-KCVZ1nJzrF5KJmtv7S_-YHMTlzHmwvjX900gbFTxg130_assertion SIO_000772 22166941 NP946386.RAB-KCVZ1nJzrF5KJmtv7S_-YHMTlzHmwvjX900gbFTxg130_provenance.
- NP946386.RAB-KCVZ1nJzrF5KJmtv7S_-YHMTlzHmwvjX900gbFTxg130_assertion wasDerivedFrom befree-2016 NP946386.RAB-KCVZ1nJzrF5KJmtv7S_-YHMTlzHmwvjX900gbFTxg130_provenance.
- NP946386.RAB-KCVZ1nJzrF5KJmtv7S_-YHMTlzHmwvjX900gbFTxg130_assertion wasGeneratedBy ECO_0000203 NP946386.RAB-KCVZ1nJzrF5KJmtv7S_-YHMTlzHmwvjX900gbFTxg130_provenance.